24 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
IMMAGE SYSTEMS TOTAL IMMUNOGLOBULIN E (IGE) REAGENT IMMAGE IGE CALIBRATOR
FDA 510(k)
FDA Class 2
·Immunology
Safco Flexible Files
FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310242103·Safco flexible files #20 21mm 6/box
APEX Revision Knee
FDA UDI
Omni Life Science, Inc.·00841690113942·PS-R Insert, Size 2 x 10mm
Max-Vac Evacuator Tips Unscented
FDA UDI
PRACTICON, INC.·00723896009819·offer two unique ends for a super low price - u...
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0142100·Trial, TLIF, 32L OB CRV 7Deg, 10mm
GLUCOMETER DEX BLOOD GLUCOSE SYSTEM (MODIFIED)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PALMO THERMOREGULATION INTERFACE ACCESSORY
FDA 510(k)
FDA Class 2
·Cardiovascular
BD VACUTAINER® BORIC ACID SODIUM BORATE/FORMATE C&S URINE TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JSM·April 25, 2018
MECHANICAL CHAIR/TRANSPORT CHAIR
FDA Adverse Event
Malfunction
·UNKNOWN·Product code INM·March 27, 2013
COUGAR XT STEERABLE GUIDEWIRE
FDA Adverse Event
Malfunction
·MEDTRONIC·Product code DQX·March 3, 2011
LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 LARGE TITANIUM LAGATING
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code FZP·March 27, 2008
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code EZL·October 30, 2024
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code EZL·November 19, 2024
MICRA
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code DYB·January 24, 2024
MICRA AV
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code PNJ·January 24, 2024
MICRA
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code PNJ·January 24, 2024
MICRA
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code PNJ·January 24, 2024
MICRA
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code PNJ·January 24, 2024
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code EZL·November 26, 2024
ARROW CVC SET: 2-LUMEN 4 FR X 5 CM
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL LLC·Product code DQY·September 10, 2024